Genome-wide screening of altered m6A-tagged transcript profiles in the hippocampus after traumatic brain injury in mice

被引:51
|
作者
Wang, Yiqin [1 ]
Mao, Jian [2 ]
Wang, Xin [3 ]
Lin, Yong [2 ]
Hou, Guoqiang [2 ]
Zhu, Jun [1 ]
Xie, Baoshu [2 ,4 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, State Key Lab Med Genom,Rui Jin Hosp, CNRS LIA Hematol & Canc,Sino French Res Ctr Life, Shanghai 200127, Peoples R China
[2] Shanghai Jiao Tong Univ, Ren Ji Hosp, Sch Med, Dept Neurosurg, Shanghai 200127, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Dept Anesthesiol, 160 Pujian Rd, Shanghai 200127, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Neurosurg, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
hippocampus; N6-methyladenosine (m6A); traumatic brain injury (TBI); MESSENGER-RNA; M(6)A; EXPRESSION; METHYLATION;
D O I
10.2217/epi-2019-0002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aim: To systematically profile RNA m6A modification landscape after traumatic brain injury (TBI) in mice. Materials & methods: Expression of m6A-related genes was detected by quantitative real-time PCR (qPCR). Expression and location of METTL3, a key component of m6A methyltransferase complex, were determined by immunostaining. Genome-wide profiling of m6A-tagged transcripts was conducted by m6A-modified RNA immunoprecipitation sequencing (m6A-RIP-seq) and RNA sequencing (RNA-seq). Results: METTL3 was downregulated after TBI. In total, 922 m6A peaks were differentially expressed as determined by m6A-RIP-seq, with 370 upregulated and 552 downregulated. In addition, we identified differentially expressed hypomethylated and hypermethylated mRNA transcripts. Conclusion: Our data provided novel information regarding m6A modification changes in the early period of TBI, which might be promising therapy targets.
引用
收藏
页码:805 / 819
页数:15
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